Publications by authors named "Flavia Privitera"

Claim this Profile
G
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Jiawan Sun, Flavia Privitera

Cell· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Camille Engel, Michaela Rendek, Jessica Assoumani, Emanuela Argilli, Francesca Ariani, Flavia Privitera

Eur J Hum Genet· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Epileptic spasms and RNA analysis in a new case of Kabuki syndrome type 2.
Flavia Privitera, Camilla Meossi, Filippo Maria Santorelli, Emanuele Bartolini

Epilepsia· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of -Related Neurological Disorders.
Matteo Baggiani, Devid Damiani, Flavia Privitera, Stefania Della Vecchia, Alessandra Tessa

Int J Mol Sci· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene.
Matteo Baggiani, Filippo Maria Santorelli, Serena Mero, Flavia Privitera, Devid Damiani

Stem Cell Res· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Flavia Privitera

medRxiv· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.
Valentina Naef, Maria Lieto, Sara Satolli, Rosa De Micco, Martina Troisi, Flavia Privitera

Ann Clin Transl Neurol· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Non-Specific Epileptic Activity, EEG, and Brain Imaging in Loss of Function Variants in : A New Case Report and Review of the Literature.
Flavia Privitera, Stefano Pagano, Camilla Meossi, Roberta Battini, Emanuele Bartolini

Genes (Basel)· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
-
-Related Phenotypes and Intellectual Disability in 5q Interstitial Deletions: A New Case and Review of the Literature.
Flavia Privitera, Flavia Piccini, Maria Paola Recalcati, Silvia Presi, Silvia Mazzola

Genes (Basel)· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygosity for neuronal ceroid lipofuscinosis predisposes to bipolar disorder.
Flavia Privitera, Maria A Trusso, Floriana Valentino, Gabriella Doddato, Chiara Fallerini

Braz J Psychiatry· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
1
13q Deletion Syndrome Involving : Characterization of a New Minimal Critical Region for Psychomotor Delay.
Flavia Privitera, Arianna Calonaci, Gabriella Doddato, Filomena Tiziana Papa, Margherita Baldassarri

Genes (Basel)· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
IQSEC2 disorder: A new disease entity or a Rett spectrum continuum?
Diego Lopergolo, Flavia Privitera, Giuseppe Castello, Caterina Lo Rizzo, Maria Antonietta Mencarelli

Clin Genet· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis